GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 14026704737359

Rüsch EndoGuide T - Intubation Aid/Tube Exchanger (UDI 14026704737359)

Manufactured by Teleflex Medical

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rüsch EndoGuide T - Intubation Aid/Tube Exchanger - Primary ID 14026704737359

Device Regulatory Overview

The Rüsch EndoGuide T - Intubation Aid/Tube Exchanger (Model/Catalog Number: 503100-000060) is a medical device manufactured by Teleflex Medical. This product is indexed under FDA Product Code / Category Classification R01030102 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0675-2017 View Full Alert →

ARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured for: Teleflex Medical, The Arrow OnControl Bone Marrow Asp...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1534-2014 View Full Alert →

CAPIO, Monodeck, Violet Monofilament Polydioxanone Suture, 1 x 48 inches (122cm) Absorbable Surgical Suture, Rx Only, Teleflex Medical. Pr...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2108-2017 View Full Alert →

WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacera...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
503100-000060
Product Code / EMDN
R01030102
Device Name
RÜSCH Endo-Guide T
Database Sync Date
2026-08-09 16:29:15

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Rüsch EndoGuide T - Intubation Aid/Tube Exchanger?

The registered manufacturer of record for Rüsch EndoGuide T - Intubation Aid/Tube Exchanger is Teleflex Medical.

What is the Primary UDI-DI identifier for Rüsch EndoGuide T - Intubation Aid/Tube Exchanger?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14026704737359.

What classification code is assigned to this device?

This device is registered under product classification code R01030102.

Similar Classification Devices (R01030102)

Other Devices by Teleflex Medical

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint